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ADA Swabs

by Albino Dias de Andrade, S.A. 426 variants

Ref 00170510101200, 00170510100875, 00170540200804, 00171010101630, 00170145450200, 00170145450400.1, 00170010101228, 00170010100423, 00170245450401, 00171010101244, 00150510201200, 00170075750898, 55100000000013, 00170210201248, 00170410100815, 00170510101206, 00170030400401, 00170220151600, 00170520150804, 00401075750400, 00500240450200, 00500510100401, 00150410100800, 00401005050400, 00170505050844, 00300075750499, 00130045450288, 00170145450438.1, 00170645450201, 00171010080810, 00170075751223, 00170010101628, 00300510100406, 00300010100423, 00300040200400, 00170010100810, 00170245450459, 00170445450401.1, 00170010100899, 00200030300821, 00170010080809, 00500410101600, 00400210200606, 00500110201600, 55100000000015, 00150510100800, 00170180110000, 00500530400201, 00200010100400, 00170105101600, 00170240200802Model Sterile gauze and non-woven dressings without XR contrast thread, Sterile gauze and non-woven dressings with XR contrast thread, ADA Swabs, Non-sterile gauze and non-woven dressings without XR contrast thread, Gauze roll

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number560082989C0102XD Basic UDI-DI Date11 Jul 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Sterile gauze and non-woven dressings
Sterile gauze and non-woven dressings (RX)
Non-sterile gauze and non-woven dressings
Bleached hydrophilic cotton gauze fabric in roll
Model / Reference
Sterile gauze and non-woven dressings without XR contrast thread, 00170510101200, Sterile gauze and non-woven dressings with XR contrast thread, 00170510100875, 00170540200804, 00171010101630, 00170145450200, 00170145450400.1, ADA Swabs, 00170010101228, Non-sterile gauze and non-woven dressings without XR contrast thread, 00170010100423, 00170245450401, 00171010101244, 00150510201200, 00170075750898, Gauze roll, 55100000000013, 00170210201248, 00170410100815, 00170510101206, 00170030400401, 00170220151600, 00170520150804, 00401075750400, 00500240450200, 00500510100401, 00150410100800, 00401005050400, 00170505050844, 00300075750499, 00130045450288, 00170145450438.1, 00170645450201, 00171010080810, 00170075751223, 00170010101628, 00300510100406, 00300010100423, 00300040200400, 00170010100810, 00170245450459, 00170445450401.1, 00170010100899, 00200030300821, 00170010080809, 00500410101600, 00400210200606, 00500110201600, 55100000000015, 00150510100800, 00170180110000, 00500530400201, 00200010100400, 00170105101600, 00170240200802
Primary DI / UDI-DI
05600829892661, 05600846260832, 05600829892814, 05600829891503, 05600829892241, 05600829890179, 15600701940340, 15600701940920, 05600829890353, 05600829894429, 05600829891459, 05600829894641, 05600846269620, 05600829896867, 05600829892500, 05600829891930, 05600216390619, 05600829892326, 05600829892722, 05600829895341, 05600216390244, 05600829890384, 05600829894320, 05600829895334, 05600829898731, 05600216390718, 05600846267725, 05600829894771, 05600829895211, 05600829896980, 15600829891296, 15600829898738, 05600829893590, 15600829899766, 05600829893361, 05600829891701, 05600829891770, 05600829896225, 05600829895976, 05600829895051, 15600829898189, 05600829893989, 05600829891367, 05600829890315, 05600846269644, 05600216390107, 05600829891756, 05600216390695, 15600701940845, 05600829890391, 05600846263000
Basic UDI-DI
560082989C0102XD, 560082989C0104XH, 560082989C0103XF, 560082989A0101WM, 560082989A0401X4, 560082989B0101WY, 560082989C0101XB
EMDN Code
M0201020101, M0201020201, M0201020202, M0201020102, M020107, M0202010101, M0202010201, M0202010102
Device Class
Class IIa
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000002823

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Properties

  • Sterile YesEUDAMEDNoEUDAMED

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No